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VION ECG Pen - Indonesia BPOM Medical Device Registration

VION ECG Pen is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502220373. The device is manufactured by MD BIOMEDICAL (FOSHAN) CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GLOBAL ENERGY ALKESINDO.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : B
VION ECG Pen
Analysis ID: AKL 20502220373

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. GLOBAL ENERGY ALKESINDO

AR Address

GLOBAL ENERGY ALKESINDO

Registration Date

Nov 11, 2022

Expiry Date

Aug 15, 2027

Product Type

Monitoring Cardiology Equipment

Electrocardiograph.

Non Radiation Electromedics

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